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Human Mutation|January 1, 1997
Tay-Sachs disease-causing mutations and neutral polymorphisms in the Hex A geneR MyerowitzProceedings of the National Academy of Sciences of the United States of America|June 1, 1988
Splice junction mutation in some Ashkenazi Jews with Tay-Sachs disease: evidence against a single defect within this ethnic groupR MyerowitzAnalytical Biochemistry|April 1, 1990
A gel electrophoretic assay for detecting the insertion defect in Ashkenazi Jewish carriers of Tay-Sachs diseaseS Shore, R MyerowitzScience (New York, N.Y.)|June 27, 1986
Different mutations in Ashkenazi Jewish and non-Jewish French Canadians with Tay-Sachs diseaseR Myerowitz, N D HogikyanThe Journal of Biological Chemistry|October 25, 1981
The mannose 6-phosphate receptor of Chinese hamster ovary cells. Compartmentalization of acid hydrolases in mutants with altered receptorsA R Robbins, R MyerowitzThe Journal of Biological Chemistry|December 15, 1988
The major defect in Ashkenazi Jews with Tay-Sachs disease is an insertion in the gene for the alpha-chain of beta-hexosaminidaseR Myerowitz, F C CostiganProceedings of the National Academy of Sciences of the United States of America|September 1, 1984
cDNA clone for the alpha-chain of human beta-hexosaminidase: deficiency of alpha-chain mRNA in Ashkenazi Tay-Sachs fibroblastsR Myerowitz, R L ProiaThe Journal of Biological Chemistry|November 15, 1987
A deletion involving Alu sequences in the beta-hexosaminidase alpha-chain gene of French Canadians with Tay-Sachs diseaseR Myerowitz, N D HogikyanBiochimica Et Biophysica Acta|February 18, 1982
Specific chemical modification of the readily nitrated tyrosine of the RTEM beta-lactamase and of bacillus cereus beta-lactamase I. The role of the tyrosine in beta-lactamase catalysisB L Wolozin, R Myerowitz, R F PrattHuman Mutation|January 1, 1992
An unusual genotype in an Ashkenazi Jewish patient with Tay-Sachs diseaseS Shore, J Tomczak, E E Grebner, et al.Pageof 2